NM_000551.4(VHL):c.261A>G (p.Val87=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002427306.2
Allele description [Variation Report for NM_000551.4(VHL):c.261A>G (p.Val87=)]
NM_000551.4(VHL):c.261A>G (p.Val87=)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
Homo sapiens UDP glycosyltransferase 8 (UGT8), transcript variant 1, mRNA
Homo sapiens UDP glycosyltransferase 8 (UGT8), transcript variant 1, mRNAgi|189491659|ref|NM_001128174.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024